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芍药苷通过依赖于核转录因子Y亚基A(NF-YA)的蛋白水解作用消除脊髓延髓性肌萎缩症中的突变雄激素受体。

Paeoniflorin eliminates a mutant AR via NF-YA-dependent proteolysis in spinal and bulbar muscular atrophy.

作者信息

Tohnai Genki, Adachi Hiroaki, Katsuno Masahisa, Doi Hideki, Matsumoto Shinjiro, Kondo Naohide, Miyazaki Yu, Iida Madoka, Nakatsuji Hideaki, Qiang Qiang, Ding Ying, Watanabe Hirohisa, Yamamoto Masahiko, Ohtsuka Kenzo, Sobue Gen

机构信息

Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.

Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan

出版信息

Hum Mol Genet. 2014 Jul 1;23(13):3552-65. doi: 10.1093/hmg/ddu066. Epub 2014 Feb 18.

Abstract

The accumulation of abnormal proteins is a common characteristic of neurodegenerative diseases. This accumulation reflects a severe disturbance of cellular homeostasis in pathogenic protein clearance. Here, we demonstrated that the activation of the two major proteolytic machineries, the molecular chaperone-ubiquitin proteasome system (UPS) and the autophagy system, were simultaneously enhanced by paeoniflorin (PF), a major component of Paeonia plants, and exerted therapeutic effects in models of spinal and bulbar muscular atrophy (SBMA). PF significantly increased the expression of nuclear factor-YA (NF-YA), which strongly upregulated the molecules involved in the proteolytic machinery [molecular chaperones, carboxyl terminus of Hsc70-interacting protein and transcription factor EB], which thus mitigated the behavioral and pathological impairments in an SBMA mouse model through the upregulation of pathogenic androgen receptor protein clearance in motor neurons and muscles. These findings demonstrated that PF is able to enhance both the UPS and autophagy systems by upregulating the expression of NF-YA, which promotes therapeutic effects in an SBMA model.

摘要

异常蛋白质的积累是神经退行性疾病的一个共同特征。这种积累反映了致病蛋白清除过程中细胞稳态的严重紊乱。在此,我们证明了芍药苷(PF),一种芍药属植物的主要成分,可同时增强两种主要的蛋白水解机制,即分子伴侣 - 泛素蛋白酶体系统(UPS)和自噬系统,并在脊髓性延髓肌萎缩(SBMA)模型中发挥治疗作用。PF显著增加了核因子 - YA(NF - YA)的表达,NF - YA强烈上调了参与蛋白水解机制的分子[分子伴侣、Hsc70相互作用蛋白的羧基末端和转录因子EB],从而通过上调运动神经元和肌肉中致病雄激素受体蛋白的清除,减轻了SBMA小鼠模型中的行为和病理损伤。这些发现表明,PF能够通过上调NF - YA的表达来增强UPS和自噬系统,从而在SBMA模型中发挥治疗作用。

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